Following consent, participants completed a baseline assessment,

Following consent, participants completed a baseline assessment, attended a presentation on HIV prevention methods, and completed

a postintervention assessment. Participants of the study were compensated for their time (1.5 to 2 hours) to complete the intervention and questionnaires, and received www.selleckchem.com/products/crenolanib-cp-868596.html $15. The estimated minimum time needed to complete study procedures was: eligibility and coordination with referring health care provider (5 minutes), informed consent process (20 minutes), baseline assessment (20 minutes), intervention (15 minutes), postintervention assessment (20 minutes), and final check, review of all forms, compensation, and receipt (10 minutes). Questionnaires Demographics and sexual risk factors This questionnaire’s topics included age, race, ethnicity, educational level, marital status, number of partners in the prior 2 months, and use of condoms in the last sexual encounter. Outcome measure: preference Self-perceived HIV risk and knowledge, and attitudes regarding traditional and new biomedical methods of HIV prevention (ie, male circumcision, PrEP, microbicides, male and female condoms, a hypothetical HIV vaccine) were assessed. Items assessed willingness to use HIV prevention methods, using a Likert scale scored 1 to 5 (5= strongly agree, 4= somewhat agree, 3= neutral, 2= somewhat disagree, and 1= strongly disagree); higher scores indicated greater willingness.

Intervention Participants were provided with information on new biomedical prevention strategies, in their preferred language. The information

was given in simple terms and included the definition of the method, and the main advantages and disadvantages of each method. It also included a representative graphic (eg, drawing of status pre- and postcircumcision, pill box, and a microbicide applicator). Participants were given the option to review the information by reading a pamphlet or by viewing a brief video (5 minutes) containing the same information. The information about each HIV prevention method was provided in a randomly alternating order to avoid ordering effect bias. The study coordinator was also available AV-951 to answer any questions about the information provided. Postintervention assessment of biomedical HIV prevention preferences used the same scales as in the baseline evaluation. Questionnaires were completed by participants, but study staff were also available to clarify questions. Data analysis Data was coded and uploaded into the Statistical Package for Social Sciences (SPSS) software for statistical analysis. Descriptive statistics were performed on the total sample and subgroups by sex, ethnicity/race, and sexual preference. Associations (chi square) between all the subgroups and preferences for the three interventions were examined. Results Demographics and HIV risk Study participants (n=97) included 51 women and 46 men. Demographic characteristics are presented in Table 1.

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